FDA approves Novartis Kymriah CAR-T cell therapy for adult patients with relapsed or refractory follicular lymphoma

Novartis

27 May 2022 - 68% of patients receiving Kymriah in the ELARA trial experienced complete response, with an 86% overall response rate, along with a remarkable safety profile.

Novartis today announced the US FDA has granted accelerated approval for Kymriah (tisagenlecleucel) for the treatment of adult patients with relapsed or refractory follicular lymphoma after two or more lines of systemic therapy.

Read Novartis press release

Michael Wonder

Posted by:

Michael Wonder

Posted in:

Cancer , Outcome , US , Cellular therapy